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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796191Generated: October 31, 2026

4-Nitrophenol → Ethyl 4-nitrophenyl carbonate

https://huagongshe.com/reaction/1796191

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-NitrophenolHCID 980—
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantEthyl chloroformateHCID 10928—
SolventDichloromethaneHCID 6344—
ProductEthyl 4-nitrophenyl carbonateHCID 58686395%

Reaction Steps

To a solution of 4-nitrophenol (1.00 g) in dichloromethane (20 ml) were added dropwise ethyl chloroformate (0.70 ml) and pyridine (0.70 ml) under ice-cooling, and the resulting mixture was stirred at room temperature overnight and then evaporated in vacuo. To the residue obtained was added ethyl acetate, and the organic layer was washed successively with a saturated aqueous sodium hydrogencarbonate solution, a saturated aqueous sodium chloride solution, a saturated aqueous potassium hydrogensulfate solution and a saturated aqueous sodium chloride solution. The organic layer was dried over anhydrous magnesium sulfate and evaporated in vacuo. The residual solid obtained was collected by filtration using hexane to afford ethyl 4-nitrophenyl carbonate (1.44 g, yield: 95%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030138B2
Source datasetuspto-grants-2006_04
ORD IDord-1f796e95d6c7409b88e9c4087a261aa3
Source noteuspto-grants-2006_04